NBPF11

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, NBPF11 Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated NBPF11 data layer compared with 23 for mass-spec protein.

The strongest signal is observed in kidney renal papillary cell carcinoma (KIRP), where higher NBPF11 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated NBPF11 expression acts as an unfavorable survival marker.

KIRP, LUSC, and UCEC are the cancer types where NBPF11 Mutation most reproducibly stratifies survival.

Mutation survival associations by lineage

Ranked by sampling consensus. AUC1 and AUC2 indicate survival in the high- and low-expression groups, respectively; the lower AUC marks the poorer-surviving group. p-values are from the log-rank test.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
KIRPDFSMedianAll0.0370.920<.00124view →
LUSCOSMedianIII,IV0.1120.664.00320view →
UCECOSMedianIV0.2250.772<.00112view →
SKCMOSMedianIII,IV0.2650.711.00110view →
PRADDFSMedianAll0.0850.774<.0016view →
COADDFSMedianAll0.2060.585.0372view →
Pink = unfavorable, green = favorable. Showing the 6 strongest of 6 lineages.

NBPF11–KIRP (DFS)

Kaplan–Meier survival curve for NBPF11 mutant vs wild-type samples in KIRP.

Open the KIRP breakdown →

Exploration